Job Description

QRC Group, LLC is a firm dedicated to offer services to the Pharmaceutical, Medical Devices and Chemical Industries in the validation and regulatory fields.

Log on now to our website http://www. qrcgroup.com to learn more about our services and solutions!

We are seeking a temporary technical resource to support Sterile Manufacturing Operations, with a focus on inspection engineering activities and parenteral inspection technologies, supporting ongoing operations, product transfers, and continuous improvement initiatives.

Key Responsibilities

• Lead inspection engineering activities
• Develop and implement new inspection technologies
• Provide support for product transfers
• Deliver operational support of inspection systems for sterile/biologic products
• Lead process improvements
• Execute validation and line trials
• Troubleshoot inspection equipment
• Manage inspection-related projects to ensure compliance, quality, and efficiency

Collaboration

• Collaborate cross-functionally with manufacturing, engineering, quality, and validation teams
• Ensure alignment with site priorities and regulatory requirements

Qualifications

• Strong technical expertise
• Problem-solving capabilities
• Experience in pharmaceutical sterile manufacturing environments

Education & Experience (Inferred Based on Industry Standards)

• Bachelor’s degree in Engineering (Mechanical, Electrical, Industrial, Chemical, or related field) or applied sciences
• Approximately 5–10+ years of experience in sterile/biologic inspection systems or inspection technologies
• Experience with validation, equipment troubleshooting, and implementation of inspection technologies

Additional Information

All your information will be kept confidential according to EEO guidelines.